Variant (rsID / SNP)

rs655415

rs655415 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR13H1. The table records no clinical significance for this variant.

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Reference-table entries

OR13H1Not classified

Variant type: missense_variant
HGVS: NM_001004486.1,c.797A>C,p.Tyr266Ser
Allele change: Missense_Y266S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.